Department of Medical Oncology, Institute of Oncology, Istanbul University, Istanbul, Turkey.
Curr Oncol. 2013 Dec;20(6):e546-53. doi: 10.3747/co.20.1596.
We investigated the prognostic clinicopathologic factors associated with overall survival (os) and progression-free survival (pfs) in the once-daily continuous administration of first-line sunitinib in a consecutive cohort of Turkish patients with metastatic renal cell carcinoma (rcc).
The study enrolled 77 Turkish patients with metastatic rcc who received sunitinib in a continuous once-daily dosing regimen between April 2006 and April 2011. Univariate analyses were performed using the log-rank test.
Median follow-up was 18.5 months. In univariate analyses, poor pfs and os were associated with 4 of the 5 factors in the Memorial Sloan-Kettering Cancer Center (mskcc) score: Eastern Cooperative Oncology Group performance status of 2 or higher, low hemoglobin, high corrected serum calcium, and high lactate dehydrogenase. In addition to those factors, hypoalbuminemia, more than 2 metastatic sites, liver metastasis, non-clear cell histology, and the presence of sarcomatoid features on pathology were also associated with poor pfs; and male sex, hypoalbuminemia, prior radiotherapy, more than 2 metastatic sites, lung metastasis, nuclear grade of 3 or 4 for the primary tumour, and the presence of sarcomatoid features were also associated with poorer os. The application of the mskcc model distinctly separated the pfs and os curves (p < 0.001).
Our study identified prognostic factors for pfs and os with the use sunitinib as first-line metastatic rcc therapy and confirmed that the mskcc model still appears to be valid for predicting survival in metastatic rcc in the era of molecular targeted therapy.
我们研究了与转移性肾细胞癌(rcc)患者一线舒尼替尼每日一次连续给药的总生存(os)和无进展生存(pfs)相关的预后临床病理因素。
本研究纳入了 77 例接受舒尼替尼连续每日一次给药方案治疗的土耳其转移性 rcc 患者,该研究于 2006 年 4 月至 2011 年 4 月进行。采用对数秩检验进行单因素分析。
中位随访时间为 18.5 个月。在单因素分析中,5 个 Memorial Sloan-Kettering Cancer Center(mskcc)评分中的 4 个因素与较差的 pfs 和 os 相关:东部合作肿瘤组(ECOG)表现状态为 2 或更高、低血红蛋白、高校正血清钙和高乳酸脱氢酶。除了这些因素外,低白蛋白血症、超过 2 个转移部位、肝转移、非透明细胞组织学和病理上存在肉瘤样特征也与较差的 pfs 相关;男性、低白蛋白血症、既往放疗、超过 2 个转移部位、肺转移、原发肿瘤核分级 3 或 4 级以及存在肉瘤样特征也与较差的 os 相关。mskcc 模型的应用明显分离了 pfs 和 os 曲线(p < 0.001)。
我们的研究确定了舒尼替尼作为一线转移性 rcc 治疗的 pfs 和 os 的预后因素,并证实 mskcc 模型在分子靶向治疗时代仍然适用于预测转移性 rcc 的生存。